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Peter Propping

Peter Propping

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Genetics
Germany
2024
Award Badge
Genetics and Molecular Biology
Germany
2024

D-Index & Metrics

Genetics

D-Index
103
Citations
42105
World Ranking
677
National Ranking
55

Medicine

D-Index
106
Citations
44156
World Ranking
6497
National Ranking
369

Research.com Recognitions

  • 2024 - Research.com Genetics in Germany Leader Award
  • 2024 - Research.com Genetics and Molecular Biology in Germany Leader Award
  • 2023 - Research.com Genetics in Germany Leader Award

Overview

Peter Propping was affiliated with the University of Bonn in Germany during their academic career. The scientist's work, as documented, did not feature listed research papers, frequent co-authors, or specific publication venues that are publicly recorded for this profile.

No information is available regarding their main fields or subfields of study, and there are no recorded main topics of their research work. Similarly, there are no details relating to book publications or awards received.

The absence of detailed bibliographic or collaborative data limits the ability to provide a comprehensive overview of scientific contributions or specific areas of expertise. Nonetheless, the association with a major European research institution such as the University of Bonn indicates an engagement with academic research in the relevant domain during their active years.

Best Publications

  • Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

    S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone

  • Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

    Pamela Sklar;Pamela Sklar;Stephan Ripke;Stephan Ripke;Laura J. Scott;Ole A. Andreassen

  • A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.

    Ortrud K. Steinlein;John C. Mulley;Peter Propping;Robyn H. Wallace;Robyn H. Wallace

  • A Potassium Channel Mutation in Neonatal Human Epilepsy

    Christian Biervert;Björn C. Schroeder;Björn C. Schroeder;Björn C. Schroeder;Christian Kubisch;Christian Kubisch;Christian Kubisch;Samuel F. Berkovic;Samuel F. Berkovic;Samuel F. Berkovic

  • Identification of loci associated with schizophrenia by genome-wide association and follow-up

    Michael C. O'Donovan;Nicholas Craddock;Nadine Norton;Hywel Williams

  • Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers.

    E G Jönsson;M M Nöthen;F Grünhage;L Farde

  • A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder.

    A E Baum;N Akula;M Cabanero;I Cardona

  • Excess of High Activity Monoamine Oxidase A Gene Promoter Alleles in Female Patients with Panic Disorder

    Jürgen Deckert;Marco Catalano;Yana V. Syagailo;Monica Bosi

  • Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

    Colm O'Dushlaine;Lizzy Rossin;Phil H. Lee;Laramie Duncan;Laramie Duncan

  • Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.

    Ricardo Segurado;Sevilla D. Detera-Wadleigh;Douglas F. Levinson;Cathryn M. Lewis

  • Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24

    Stefanie Birnbaum;Stefanie Birnbaum;Kerstin U Ludwig;Heiko Reutter;Stefan Herms

  • Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

    Elisabeth Mangold;Kerstin U. Ludwig;Stefanie Birnbaum;Carlotta Baluardo

  • Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444

    Reiner Caspari;Sylciane Olschwang;Waltraut Friedl;Marion Mandl

  • Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

    Bryony A Thompson;Bryony A Thompson;Amanda B Spurdle;John-Paul Plazzer;Marc S Greenblatt

  • The electroencephalogram (EEG) as a research tool in human behavior genetics: psychological examinations in healthy males with various inherited EEG variants. I. Rationale of the study. Material. Methods. Heritability of test parameters.

    F Vogel;E Schalt;J Krüger;P Propping

  • Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies

    Karsten Haug;Maike Warnstedt;Alexi K Alekov;Thomas Sander

  • Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder.

    J Schumacher;R Abon Jamra;J Freudenberg;T Becker

  • An Insertion Mutation of the CHRNA4 Gene in a Family With Autosomal Dominant Nocturnal Frontal Lobe Epilepsy

    Ortrud K. Steinlein;Andres Magnusson;Jens Stoodt;Sonia Bertrand

  • Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families

    W Friedl;R Caspari;M Sengteller;S Uhlhaas

  • Expanded Extracolonic Tumor Spectrum in MUTYH-Associated Polyposis

    Stefanie Vogt;Natalie Jones;Daria Christian;Christoph Engel

Frequent Co-Authors

Markus M. Nöthen
Markus M. Nöthen University Hospital Bonn
Sven Cichon
Sven Cichon University of Basel
Marcella Rietschel
Marcella Rietschel Heidelberg University
Wolfgang Maier
Wolfgang Maier University of Bonn
Johannes Schumacher
Johannes Schumacher Philipp University of Marburg
Thomas G. Schulze
Thomas G. Schulze Ludwig-Maximilians-Universität München
Rami Abou Jamra
Rami Abou Jamra Leipzig University
Tim Becker
Tim Becker University of Bonn
Michael Knapp
Michael Knapp University of Bonn
Elisabeth Mangold
Elisabeth Mangold University of Bonn

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